The nurse should prioritize Phenylketonuria in further assessments to rule out.
What is Phenylketonuria?
Phenylketonuria or PKU, is a rare, inherited birth defect that causes phenylalanine, an amino acid, to build up in the body. Phenylketonuria is caused due to a change in the phenylalanine hydroxylase (PAH) gene. The phenylalanine hydroxylase (PAH) gene helps create the enzyme that is needed for breakdown of phenylalanine.
There are no symptoms to PKU, if treated early. Without treatment, it can lead to brain damage and damage to the nervous system, which may lead to learning disabilities.
Other symptoms of untreated Phenylketonuria are behavioural difficulties such as episodes of self-harm and frequent temper tantrum.
Therefore, the nurse should prioritize Phenylketonuria in further assessments to rule out.
Learn more about Phenylketonuria here: https://brainly.com/question/11443201
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